drugset / Trial / NCT03187756

Study of Nonmyeloablative Peripheral Blood Stem Cell Transplant With High-dose Posttransplantation Cyclophosphamide in Hematopoietic Malignancies Including Those That Are Challenging to Engraft

NCT03187756 ↗

Phase 2 Terminated 6 enrolled NYU Langone Health
NaSingle-groupOpen-labelTreatment

Summary

This is an open label phase II single arm study of peripheral blood stem cell transplantation and posttransplantation cyclophosphamide, using HLA full match or haploidentical related donors, in hematological malignancies including those difficult to engraft. The objective of this study is to evaluate the safety and feasibility in nonmyeloablative, partially HLA-mismatched or HLA-matched PBSC transplant from haploidentical donors or fully matched donors with post-grafting immunosuppression that includes high-dose cyclophosphamide, tacrolimus, and Mycophenolate mofetil (MMF).

Timeline

Start
2017-06-02
Primary completion
2018-12-18
Completion
2018-12-18

Outcome

Outcome not reported

Stopped: “Procedure has become standard of care - protocol is no longer necessary”

Drugs

EvaluationDrugModalityDoseRoute
Subject Cyclophosphamide Other / unclassified — —